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Clinical implications of genetic advances in Charcot–Marie–Tooth disease

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Year: 2013
Type: review
Source: Nature Reviews Neurology
DOI: 10.1038/nrneurol.2013.179
Authors: Alexander M. Rossor, James M. Polke, Henry Houlden, Mary M. Reilly
Institutions: National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology, University College London
Language: English

Topic: Hereditary Neurological Disorders
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institute for Health and Care Research, Medical Research Council, National Institute of Neurological Disorders and Stroke
Awards: MICA: MRC Centre for Neuromuscular Diseases, The Inherited Neuropathy Consortium (INC) RDCRC- Overall, Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study
OpenAlex ID: W1965759164
FWCI: 3.546
Cites: 32
Cited by: 362
Related to: 10
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